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Interleukin-1-mediated effects of normal oral keratinocytes and head and neck squamous carcinoma cells on extracellular matrix related gene expression in fibroblasts

Hakelius, Malin (författare)
Uppsala universitet,Plastikkirurgi
Koskela, Anita (författare)
Clinical Research Center, University Hospital, Örebro, Sweden
Reyhani, Vahid (författare)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
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Ivarsson, Mikael, 1962- (författare)
Örebro universitet,Institutionen för hälsovetenskap och medicin,Clinical Research Center, University Hospital, Örebro, Sweden
Grenman, Reidar (författare)
Department of Otorhinolaryngology-Head and Neck Surgery and Medical Biochemistry, Turku University Hospital, University of Turku, Turku, Finland
Rubin, Kristofer (författare)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
Gerdin, Bengt (författare)
Uppsala universitet,Plastikkirurgi
Nowinski, Daniel (författare)
Uppsala universitet,Plastikkirurgi
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 (creator_code:org_t)
Elsevier, 2012
2012
Engelska.
Ingår i: Oral Oncology. - : Elsevier. - 1368-8375 .- 1879-0593. ; 48:12, s. 1236-1241
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Objectives: The composition of tumor stroma and the activity of tumor associated fibroblasts are important for tumor growth. Interactions between carcinoma cells and fibroblasts regulate the turnover of extracellular matrix (ECM). Here, the in vitro effects of oral squamous cell carcinoma (SCC) cells (UT-SCC-30 and UT-SCC-87) on fibroblast expression of genes for ECM components and connective tissue growth factor (CTGF/CCN2), were compared to those of normal oral keratinocytes (NOK).Materials and Methods: Cocultures with fibroblasts in collagen gels and keratinocytes with the two cell types separated by a semi permeable membrane were used, and relative gene expression was measured with real-time PCR.Results: All investigated genes were regulated by NOK and the SCCs. The downregulation of pro-collagens alpha 1(I) and alpha 1(III) was more pronounced in cocultures with NOK, while the expression of CCN2 and fibronectin was downregulated by both NOK and the SCCs to a similar extent. UT-SCC-87, but not UT-SCC-30, secreted significantly more IL-1 alpha than NOK. A recombinant interleukin-1 receptor antagonist reversed many of the observed effects on fibroblast gene expression suggesting involvement of IL-1 in cocultures with NOK as well as with SCCs.Conclusion: The observed differential effects on fibroblast gene expression suggest that NOK are more antifibrotic compared to UT-SCC-30 and UT-SCC-87. These findings may contribute to a better understanding of the mechanisms behind ECM turnover in tumors. (C) 2012 Elsevier Ltd. All rights reserved.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Odontologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Dentistry (hsv//eng)

Nyckelord

Cocultures
Extracellular matrix
Interleukin-1 alpha
Tumor stroma
Onkologi
Oncology

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ref (ämneskategori)
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